Longer than you see here, with details, pix, and sauce.

https://jessicar.substack.com/p/bombshell-findings-from-an-fda-supervised

. . . These students demonstrate innovative thinking, fantastic deployment of their ideas, and excellent writing and figure-production skills. To me, their work demonstrates a far higher quality level than we have seen emerge from other labs - including exceedingly well (pharma)-funded labs - and this begs a very important question.

If these high school students can easily demonstrate DNA in commercial product vials (and these included XBB vials - later production) that were injected into billions of people, why can’t the manufacturers and regulators seem to after 3 years?

And furthermore, when the regulators (HC, TGA, specifically) were apprised of these findings from a multitude of labs from around the world, why did they underplay the importance and relevance of replication-competent foreign DNA in the vials, especially when SV40 promoter/enhancer is among them? The TGA in fact referred to our work as “misinformation”.

Perhaps the most damning point here - beyond the kids’ ingenious methods and findings that confirm current fundings on this subject matter - is that the FDA as an agency chose not to make these findings public. The students were under the supervision of FDA employees. I mean, I can’t imagine that if they were indeed being provided technical support and materials that their work was not being monitored and supervised by the cited FDA members. I am not pointing specific fingers (I do understand that there is pressure to be “quiet” and I applaud the FDA members cited in the paper for allowing this study to be done!), but if these were my students, I would have brought these findings to the FDA head, and if I was ignored, I would have brought it to the non-legacy media.

This is an issue that involves all of us and it could have serious implications. Or perhaps not. But the only way to find out whether we are dealing with a serious problem is to first:

1- admit there’s a problem and then

2- tackle the problem by further investigating the problem.

The people have a right to know.

We need to follow-up on these findings. We need to test people’s cells for stable integration. We need to test biopsies from tumors in people post injection. We need proper controls. We don’t have a working methodology to determine whether or not a rabid stage 4 cancer, for example, was the by-product of someone being introduced to billions of fragments of foreign DNA from the modRNA-LNP injections. We need to establish such a methodology. We need the regulatory bodies - or rather, the non-compromised individuals left working for these agencies - to step up and do their jobs. And we need to impose a moratorium on this platform immediately, prior to any more injection regimens going ahead that involve them.

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